Canonical Allele Identifier: CA4800490
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs754157534
gnomAD v2: 8-87751852-T-A
gnomAD v3: 8-86739624-T-A
gnomAD v4: 8-86739624-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739624T>A , CM000670.2:g.86739624T>A GRCh38
NC_000008.10:g.87751852T>A , CM000670.1:g.87751852T>A GRCh37
NC_000008.9:g.87820968T>A NCBI36
NG_016980.1:g.9052A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.211+31A>T MANE Select ENSP00000316605.5:n.211+31A>T
ENST00000681746.1:c.211+31A>T ENSP00000505959.1:n.211+31A>T
ENST00000320005.5:c.211+31A>T ENSP00000316605.5:n.211+31A>T
ENST00000519777.1:n.193+31A>T
NM_019098.4:c.211+31A>T NP_061971.3:n.211+31A>T
NM_019098.5:c.211+31A>T MANE Select NP_061971.3:n.211+31A>T